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BRG1 regulation by miR-155 in human leukemia and lymphoma cell lines
Cuadros, M; Sánchez-Martín, V; Herrera, A; Baliñas, C; Martín-Padrón, J; Boyero, L; Peinado, P; Medina, PP.
Afiliação
  • Cuadros, M; University of Granada. Department of Biochemistry and Molecular Biology III and Immunology. Granada. Spain
  • Sánchez-Martín, V; University of Granada. Department of Biochemistry and Molecular Biology III and Immunology. Granada. Spain
  • Herrera, A; GENYO, Centre for Genomics and Oncological Research. Granada. Spain
  • Baliñas, C; GENYO, Centre for Genomics and Oncological Research. Granada. Spain
  • Martín-Padrón, J; University of Granada. Department of Biochemistry and Molecular Biology III and Immunology. Granada. Spain
  • Boyero, L; University of Granada. Department of Biochemistry and Molecular Biology III and Immunology. Granada. Spain
  • Peinado, P; GENYO, Centre for Genomics and Oncological Research. Granada. Spain
  • Medina, PP; GENYO, Centre for Genomics and Oncological Research. Granada. Spain
Clin. transl. oncol. (Print) ; 19(8): 1010-1017, ago. 2017. tab, `bgraf, ilus
Artigo em Inglês | IBECS | ID: ibc-164679
Biblioteca responsável: ES1.1
Localização: BNCS
ABSTRACT
Introduction/purpose. BRG1 is a key regulator of leukemia stem cells. Indeed, it has been observed that this type of cells is unable to divide, survive and develop new tumors when BRG1 is down-regulated. Materials and methods. We assessed BRG1 and miR-155 expression in 23 leukemia cell lines, and two no pathological lymphocyte samples using qPCR. MiR-155 transfection and western blot were used to analyze the relationship between miR-155 and its validated target, BRG1, by measuring protein expression levels. The effect of miR-155 on cell proliferation and prednisolone sensitivity were studied with resazurin assay. Results. BRG1 expression levels could correlate negatively with miR-155 expression levels, at least in Burkitt’s lymphoma and diffuse large B cell lymphoma (DLBCL) cell lines. To clarify the role of miR-155 in the regulation of BRG1 expression, we administrated miR-155 mimics in different leukemia/lymphoma cell lines. Our results suggest that miR-155 regulate negatively and significantly the BRG1 expression at least in the MOLT4 cell line. Conclusion. Our study revealed a previously unknown miR-155 heterogeneity that could result in differences in the treatment with miRNAs in our attempt to inhibit BRG1. However, the expression levels of BRG1 and miR-155, before prednisolone treatment were not statistically significantly associated prednisolone sensitive leukemia cells (AU)
RESUMEN
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Assuntos
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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Prednisolona / Leucemia Linfocítica Crônica de Células B / MicroRNAs / Linhagem Celular Tumoral Tipo de estudo: Estudo diagnóstico Limite: Humanos Idioma: Inglês Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Artigo Instituição/País de afiliação: GENYO, Centre for Genomics and Oncological Research/Spain / University of Granada/Spain
Buscar no Google
Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Prednisolona / Leucemia Linfocítica Crônica de Células B / MicroRNAs / Linhagem Celular Tumoral Tipo de estudo: Estudo diagnóstico Limite: Humanos Idioma: Inglês Revista: Clin. transl. oncol. (Print) Ano de publicação: 2017 Tipo de documento: Artigo Instituição/País de afiliação: GENYO, Centre for Genomics and Oncological Research/Spain / University of Granada/Spain
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